Fluorometric study of rabbit sperm head membrane phospholipid asymmetry during capacitation and acrosome reaction using annexin-v FITC

被引:11
作者
Avalos-Rodríguez, A
Ortíz-Muñiz, R
Ortega-Camarillo, C
Vergara-Onofre, M
Rosado-García, A
Rosales-Torres, AM
机构
[1] Univ Autonoma Metropolitana, Unidad Xochimilco, Dept Prod Agricola & Anim, Lab Bioquim Reprod,Div CBS UAM Xochlzt, Mexico City 04960, DF, Mexico
[2] Univ Autonoma Metropolitana, Dept Biol Expt, Lab Biol Celular & Citometria Flujo, Unidad Iztapalapa, Mexico City, DF, Mexico
[3] Hosp Especialidades Ctr Med La Raza, Unidad Invest Med Bioquim, Inst Mexicano Seguro Social, CMN sXXI, Mexico City, DF, Mexico
[4] Univ Autonoma Metropolitana, Lab Bioquim Reprod, Dept Prod Agricola & Anim, Unidad Xochimilco, Mexico City, DF, Mexico
[5] Univ Autonoma Metropolitana, Lab Manejo Gametos, Dept Reprod Biol, Unidad Iztapalapa, Mexico City, DF, Mexico
来源
ARCHIVES OF ANDROLOGY | 2004年 / 50卷 / 04期
关键词
acrosome; Annexin-V; asymmetry; capacitation; FITC; fluorometric; phospholipid; reaction;
D O I
10.1080/01485010490448741
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
This study was conducted to evaluate phosphatidylserine translocation in head plasma membrane of Percoll-gradient purified of rabbit cauda epididymal sperm during capacitation and acrosome reaction (AR) using Annexin-V. Propidium iodide was used as control to reject dead or dying cells. The presence and distribution of Annexin-V binding sites were analyzed using flow fluorocytometry and confocal microscopy. After 6h of incubation of sperm in capacitation medium, the number of cells positively stained with Annexin-V showed a small but significant increment. The Annexin-V binding sites produced during capacitation were found mainly in the post-acrosomal region of the sperm head plasma membrane. After AR induction with progesterone, the localization of phosphatidylserine was changed and the Annexin-V binding sites were found almost only in the acrosomal region, but with higher number of binding sites in the equatorial area. On the contrary, after AR induction with A23187, phosphatidylserine translocation, although predominant over the acrosomal region, was also observed in the post-acrosomal region. Plasma membrane destabilization during capacitation and AR may be important for sperm-oocyte fusion.
引用
收藏
页码:273 / 285
页数:13
相关论文
共 32 条
[1]  
ALLEN CA, 1995, J CELL SCI, V108, P767
[2]   Mechanism of granulosa cell death during follicular atresia depends on follicular size [J].
Alonso-Pozos, I ;
Rosales-Torres, AM ;
Avalos-Rodríguez, A ;
Vergara-Onofre, M ;
Rosado-García, A .
THERIOGENOLOGY, 2003, 60 (06) :1071-1081
[3]  
Baldi E, 1996, FRONT BIOSCI, V1, P189
[4]   Mammalian fertilization misread? Sperm penetration of the eutherian zona pellucida is unlikely to be a lytic event [J].
Bedford, JM .
BIOLOGY OF REPRODUCTION, 1998, 59 (06) :1275-1287
[5]   The biochemistry of the acrosome reaction [J].
Breitbart, H ;
Spungin, B .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (03) :195-202
[6]   The human sperm acrosome reaction: Physiology and regulatory mechanisms: An update [J].
Brucker, C ;
Lipford, GB .
HUMAN REPRODUCTION UPDATE, 1995, 1 (01) :51-62
[7]   Caspase-independent exposure of aminophospholipids and tyrosine phosphorylation in bicarbonate responsive human sperm cells [J].
de Vries, KJ ;
Wiedmer, T ;
Sims, PJ ;
Gadella, BM .
BIOLOGY OF REPRODUCTION, 2003, 68 (06) :2122-2134
[8]   Capacitation as a regulatory event that primes spermatozoa for the acrosome reaction and fertilization [J].
deLamirande, E ;
Leclerc, P ;
Gagnon, C .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (03) :175-194
[9]   CA2+-REGULATING MECHANISMS THAT MODULATE BULL SPERM CAPACITATION AND ACROSOMAL EXOCYTOSIS AS DETERMINED BY CHLORTETRACYCLINE ANALYSIS [J].
FRASER, LR ;
ABEYDEERA, LR ;
NIWA, K .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 40 (02) :233-241
[10]   Capacitation induces cyclic adenosine 3′,5′-monophosphate-dependent, but apoptosis-unrelated, exposure of aminophospholipids at the apical head plasma membrane of boar sperm cells [J].
Gadella, BM ;
Harrison, RAP .
BIOLOGY OF REPRODUCTION, 2002, 67 (01) :340-350